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  • EMA’s PRAC to review Xeljanz and recommends fenspiride withdrawl pharmatimes
    May 20, 2019
    The European Medicines Agency’s (EMA) Pharmacovigilance Risk Assessment Committee (PRAC) has announced its latest meeting highlights, including a restriction of the use of Xeljanz (tofacitinib), and a call for withdrawal of marketing authorisations for fe

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